"Ambry Genetics"[submitter] AND "GRAP"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2519138	NM_006613.4(GRAP):c.590G>A (p.Arg197Gln)	GRAP, SLC5A10 (R197Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2220557	NM_006613.4(GRAP):c.533G>C (p.Ser178Thr)	GRAP, SLC5A10 (A122P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2226091	NM_006613.4(GRAP):c.479C>T (p.Ala160Val)	GRAP, SLC5A10 (A160V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3282607	NM_006613.4(GRAP):c.445C>A (p.Arg149Ser)	GRAP (R149S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3282606	NM_006613.4(GRAP):c.406C>T (p.Arg136Cys)	GRAP (R136C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102201	NM_006613.4(GRAP):c.344C>T (p.Ser115Leu)	GRAP (S115L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar